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Monthly Archives: October 2019
Dad who called on the public for stem cells for his son is up for an award – Chronicle Live
Posted: October 31, 2019 at 6:45 pm
Doting dad Stephen Armstrong knows all too well what its like to be waiting for a transplant donor.
His son Jacob was diagnosed at two years old with a rare blood disorder and called on the public to donate stem cells to find him a match.
He then set out to raise as much money as he could for the blood cancer charity Anthony Nolan in a bid to save lives.
And now, after raising over 20,000, his efforts have been recognised by the charity as they honour him at an awards ceremony held at the Tower of London in November.
Stephen, 33, of Wallsend, North Tyneside, has been shortlisted for the Individual Fundraiser of the Year Award at the Anthony Nolan Supporter Awards 2019.
The prestigious awards are back for their seventh year and will recognise the outstanding achievements of the volunteers, fundraisers and campaigners who help the pioneering blood cancer charity save lives.
Stephens nomination is in recognition of his incredible fundraising efforts, leading a group of 19 friends and family in a series of physical challenges, all while his son was undergoing treatment.
After Jacob was diagnosed in 2017, Stephen set out to find a matching stem cell donor, as well as raise awareness of the need for more people on the register.
From here Jacobs Journey was born, and through a series of challenges including the Great North Run, the Great North Bike Ride and climbing Ben Nevis, Stephen has helped raise over 20,000 for the charity.
Jacob, who turns four in November, and his family have been told he does not need a transplant, but Stephen and his family want to continue raising awareness for others who arent so lucky.
When Jacob was diagnosed, we were stunned by how few people were on the stem cell donor register. I couldnt believe how a stranger in the street could potentially save our little boys life, said Stephen, an assistant manager for Dixons Carphone.
Anthony Nolan helped us massively while Jacob was ill and provided a great support network. I feel very proud to be nominated for an award, and I hope it can help build even more awareness for the cause.
Stephen and mum Kirsty, 28, received the news in December 2017 that Jacob was suffering from bone marrow failure, which affects between 30 and 40 children each year.
They first became concerned about his health when they went abroad to get married and noticed he was getting bruised easily. The marks would take weeks to disappear, so when the couple returned to the UK they decided to take Jacob to the doctor for a check up.
After tests he was then diagnosed and was treated at the Great North Childrens Hospital in Newcastle, where he received two blood transfusions.
Stephen added: When we were told Jacob did not need the transplant it was the best news in the world, a total relief. He still needs check ups every three months and his consultants is keeping an eye on him. There are so few people on the stem cell donor register so I just wanted to create a ripple effect with awareness and get more people on it.
Stephen, who has raised a further 8,000 for other smaller charities, has also been nominated for our Chronicle Champions Award in the Champion Fundraiser category.
Henny Braund, Chief Executive of Anthony Nolan, said: It is remarkable to see how many people support our work to find a match for those in need of a stem cell transplant. Without them, none of our lifesaving work would be possible.
Stephen has shown tremendous commitment to Anthony Nolan by continually going above and beyond in his fundraising efforts.
Henny added: We want to extend a huge congratulations to Stephen and look forward to celebrating with him at the awards.
The awards take place on Thursday 28 November at the Tower of London, and all winners will be revealed on the night.
Anthony Nolan is the charity that finds matching stem cell donors for people with blood cancer and blood disorders and gives them a second chance at life. It also carries out ground-breaking research to save more lives and provide information and support to patients after a stem cell transplant, through its clinical nurse specialists and psychologists, who help guide patients through their recovery.
To see the full shortlist, and find out more about the charity visit http://www.anthonynolan.org/awards
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AgeX Therapeutics and Juvenescence Publish Paper on Engineering Strategies for Universal Cells and Provide in Vivo Observation on Immunotolerance…
Posted: October 31, 2019 at 6:45 pm
This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20191030005329/en/
In addition, the paper presents a previously unpublished in vivo observation on allogeneic human pluripotent stem cells (hPSCs) modified with AgeXs proprietary immunotolerance technology, UniverCyteTM. In humanized mice (those with a functional human immune system), UniverCyte-positive hPSCs formed larger and heavier tissue compared to controls. This observation provides support for the premise that UniverCyte-expressing tissue was potentially hypoimmunogenic and might have escaped recognition by a functional human immune system and continued to grow. Further work is required to substantiate this preliminary in vivo finding.
Hypoimmunogenic allogeneic cells are the Holy Grail in regenerative medicine, and a number of accomplished researchers have made great strides toward engineering them over the last few years, commented Dr. Nafees Malik, Chief Operating Officer at AgeX, Head of Cell & Gene Therapy at Juvenescence (a major investor in AgeX), and lead author on the paper. This is a huge area of focus for us at AgeX, via our UniverCyte technology platform. In support of our own research and as a service to the overall field, we decided to put together this paper, analyzing all the leading strategies to engineer universal cells and encapsulating them in one paper.
Dr. Maliks co-authors on the paper are Gregory Bailey, MD, Chairman of the Board of Directors of AgeX and CEO of Juvenescence; Annalisa Jenkins, MBBS, FRCP, who serves on the Board of Directors of AgeX; and Jim Mellon, Chairman of Juvenescence.
Mr. Mellon added, AgeXs UniverCyte technology platform will not only be important to the company in developing in-house therapies, it may also be transformative for the wider cell therapy industry via collaborations and licensing deals. It is quite conceivable that in the near future, allogeneic cell therapies may potentially need to be universal to be clinically and commercially competitive.
AgeX is developing its UniverCyte technology platform at its new 15,700-square-feet R&D facility, in the San Francisco Bay Area, which has current good manufacturing practices (cGMP)-capable manufacturing capacity.
Universal cells would help us and others to fulfill the original vision of cell therapy, said Dr. Bailey. Thus, I am pleased that my colleagues at AgeX and Juvenescence have put together this paper, as it should be of considerable benefit to researchers, possibly enabling them to accelerate their progress. He added, AgeXs UniverCyte technology uses a novel, modified form of the tolerogenic molecule HLA-G, which in nature plays a key role in preventing a mother from rejecting her semi-allogeneic baby.
The paper is being published online ahead of print on Wednesday, October 30, 2019. It may be found here.
About AgeX Therapeutics
AgeX Therapeutics, Inc. (NYSE American: AGE) is focused on developing and commercializing innovative therapeutics for human aging. Its PureStem and UniverCyte manufacturing and immunotolerance technologies are designed to work together to generate highly-defined, universal, allogeneic, off-the-shelf pluripotent stem cell-derived young cells of any type for application in a whole host of diseases with a high unmet medical need. AgeX has two preclinical cell therapy programs: AGEX-VASC1 (vascular progenitor cells) for tissue ischemia and AGEX-BAT1 (brown fat cells) for Type II diabetes. AgeXs revolutionary longevity platform named induced Tissue Regeneration (iTR) aims to unlock cellular immortality and regenerative capacity to reverse age-related changes within tissues. AGEX-iTR1547 is an iTR-based formulation in preclinical development. HyStem is AgeXs delivery technology to stably engraft PureStem cell therapies and slowly release iTR molecules in the body. AgeX is developing its core product pipeline for use in the clinic to extend human healthspan and is seeking opportunities to form licensing and partnership agreements around its broad IP estate and proprietary technology platforms for non-core clinical applications.
For more information, please visit http://www.agexinc.com or connect with the company on Twitter, LinkedIn, Facebook, and YouTube.
About Juvenescence
Juvenescence is a life sciences company developing therapies to increase healthy human longevity. It was founded by Jim Mellon, Dr. Greg Bailey and Dr. Declan Doogan. The Juvenescence team are highly experienced drug developers, entrepreneurs and investors with a significant history of success in the life sciences sector. Juvenescence will create, partner with or invest in new companies with longevity-related therapeutics, by in-licensing compounds from academia and industry, or forming joint ventures to develop therapeutics for longevity. Juvenescence believes that recent advances in science have greatly improved our understanding of the biology of aging and seeks to develop therapeutics with the possibility of slowing, halting or potentially reversing elements of aging.
Forward-Looking Statements
Certain statements contained in this release are forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Any statements that are not historical fact including, but not limited to statements that contain words such as will, believes, plans, anticipates, expects, estimates should also be considered forward-looking statements. Forward-looking statements involve risks and uncertainties. Actual results may differ materially from the results anticipated in these forward-looking statements and as such should be evaluated together with the many uncertainties that affect the business of AgeX Therapeutics, Inc. and its subsidiaries, particularly those mentioned in the cautionary statements found in more detail in AgeXs reports filed with the Securities and Exchange Commissions (copies of which may be obtained at http://www.sec.gov). Subsequent events and developments may cause these forward-looking statements to change. AgeX specifically disclaims any obligation or intention to update or revise these forward-looking statements as a result of changed events or circumstances that occur after the date of this release, except as required by applicable law.
View source version on businesswire.com: https://www.businesswire.com/news/home/20191030005329/en/
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Charley Webb reveals emotional reason she stored son Aces stem cells as fans thank her for educating them – OK! magazine
Posted: October 31, 2019 at 6:45 pm
Emmerdales Charley Webb has revealed that she and her co-star husband Matthew Wolfenden stored the stem cells of their youngest son, Ace.
The Debbie Dingle actress and Matthew, who plays David Metcalfe on Emmerdale, opened up on their decision in case they need the stem cells in future for a treatment.
In an emotional post, Charley, 31, said that she hopes they never need to use the stem cells, but are glad they are stored if they need the.
The mum-of-three shared a gorgeous picture of Ace in his cot as she wrote: We decided to store Aces stem cells. As parents every single one of us wants to do whats best for our children.
When I was pregnant, I heard about the possibility of collecting and storing my baby's umbilical cord stem cells, which could then be used in the future should they be needed for treatment (I hope with every part of me we never need it).
After researching, we learned that the baby's umbilical cord is a valuable source of stem cells, and these cells can be collected at birth and stored. These could then be used as a crucial part of treating or curing an illness.
Currently, there are over 80 diseases cord blood stem cells can treat.
I decided to use Smart Cells to store the stem cells: the process was easy (genuinely) and they organised everything.
Like I said, we hope we never need to use them, but it's comforting to know that we have them stored if we ever do. This is a once in a lifetime opportunity, and Im so grateful we were able to do this. Xx.
Many of Charleys fans told her that they too have made the decision to store their babies stem cells, while others thanked her for sharing the knowledge.
One person said: Wow Ive never heard of this thanks for sharing.
Another said: Amazing. Such an important thing and I think every parent should consider doing this it may save a life, so much respect for you. And ace is so cute.
And a third commented: Wow! Never knew you could do this! Great idea!
Along with baby Ace Gene, Charley who has hit out at parenting trolls is also mum to sons Buster, nine, and Bowie, three.
Bowie recently had his sweet long hair cut shorter, which resulted in Charley having to address the reasons for his hair cut on her Instagram account.
Taking to her Instagram stories, Charley denied that Bowies hair cut was a result of negative comments from trolls about the length of his hair.
Speaking to the camera, she said: "I can't believe how many messages I've had asking if I've cut Bowie's hair because of negative comments on Instagram or online.
"No! The answer to that is no. If I was cutting my child's hair because people were being negative that would be very worrying."
Revealing the real reason behind Bowies new look, Charley said: "He had it cut because he saw a picture of short hair that was all different colours like red, yellow, blue, and he wanted it to look like that and he thought it would change colour.
Obviously it didn't but he still has the hair, so it's fine."
Charley had shared a cute snap of Bowie pulling on tassels on his knitted hat which is slightly tilted to show part of his new, shorter do before she defended the chop.
She said in the caption of the snap: Hair cut=cute face visible. Bowie 3 years and 10 months. [sic]
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Some animals pause their own pregnancies, but how they do it is still a mystery – The Conversation AU
Posted: October 31, 2019 at 6:45 pm
Putting your pregnancy on pause until the time is right to give birth sounds like something out of a sci-fi novel, but for many mammals whats known as embryonic diapause is an essential part of raising their young.
Although scientists have known since the 1850s that some animals have this ability, it is only now becoming clear how it could teach us valuable lessons about human pregnancy, stem cells, and cancer.
More than 130 species of mammal can pause their pregnancies. The pause can last anywhere between a couple of days and 11 months. In most species (except some bats, who do it a little later) this happens when the embryo is a tiny ball of about 80 cells, before it attaches to the uterus.
Its not just a single group of mammals, either. Various species seem to have developed the ability as needed to reproduce more successfully. Most carnivores can pause their pregnancies, including all bears and most seals, but so can many rodents, deer, armadillos, and anteaters.
Read more: What marsupials taught us about embryo implantation could help women using IVF
More than a third of the species that take a breather during gestation are from Australia, including some possums and all but three species of kangaroo and wallaby.
The record-holder for pregnancy pause time is the tammar wallaby, which has been studied extensively for its ability to put embryos on hold for up to 11 months.
The main advantage to pausing pregnancy is that it separates mating and birth. There are two main ways in which animals do this.
The first way is to mate soon after giving birth, to have a backup pregnancy in case something happens to the newborn young. The stress of lactating triggers a pause that lasts during suckling, and the pregnancy restarts once the young leave.
The second way is to pause every pregnancy until the time is right (usually depending on the season). For example, minks mate around the start of March but put the embryos on pause until after the spring equinox (March 21), when the days are growing longer in their northern hemisphere homes. This ensures that the young are born in spring when conditions improve, and not in winter.
The tammar wallaby combines these two methods (suckling in the first half of the year, short days in the second) to pause for almost a year and give birth in January. This ensures the young leave the pouch the following spring instead of in the middle of a hot Australian summer.
Diapause was first identified in 1854 after hunters in Europe noticed that pregnancy in roe deer seemed to last a lot longer than normal. Since then scientists have been fascinated by this process and it has helped us understand more about basic reproductive processes in all mammals.
But it took until 1950 before our knowledge of pregnancy had increased enough so that we could confirm what the hunters had observed 100 years earlier.
But how the process worked at the molecular level is still a mystery. Until recently, there seemed to be no connection between which species used it and which didnt and there didnt seem to be a unifying mechanism for how pregnancy was paused. Even the hormones controlling diapause are different between mammal groups.
However, research now suggests that regardless of what hormones affect the uterus, the molecular signalling between the uterus and the embryo is conserved, at least between the mouse, mink and tammar wallaby.
Furthermore, researchers in Poland paused embryos from sheep (a non-diapause species) by transferring them into a mouse uterus and then back into the sheep with no ill effects.
This indicates the potential for diapause could lie in all mammals, including humans.
Its unlikely that pausing pregnancy will become the norm in humans. For starters, youd have to know you were pregnant within five days of conceiving to match the time when most species start diapause.
Understanding how mammals pause their pregnancies does have significant implications for our understanding of how to make healthy embryos. The time when the embryo enters into diapause is the same time in IVF when an embryo is transferred into the uterus. Diapause could help us improve how we grow embryos in culture or how to recognise which is the best embryo to transfer.
Read more: Explainer: what are stem cells?
Diapause could also help create better stem cells and find new cancer treatments. The first stem cells ever isolated by scientists came from a mouse embryo in diapause, when the cell cycle of the embryo is arrested. Stem cells are also remarkably similar to a diapaused embryo.
So understanding how diapause works at the molecular level could lead to new therapies to halt cell division or to identify markers for tumour stem cells, which are thought to be responsible for metastasis in cancer.
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Some animals pause their own pregnancies, but how they do it is still a mystery - The Conversation AU
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Restore your crowning glory with recombinant DNA tech – The New Paper
Posted: October 31, 2019 at 6:45 pm
Hair care is being taken to the next level, by utilising recombinant DNA technology to restore one's confidence and crowning glory.
Such hair restoration products or treatments are made using recombinant DNA - or DNA cloning - where selected pieces of DNA from different organisms are combined to construct artificial DNA.
At Ageless Medi-Aesthetics, its latest AnteAge MD Hair Treatment is a non-invasive procedure that involves applying the AnteAge MD Hair Growth Factor solution or serum - made from potent recombinant growth factors and cytokines - onto skin prepared with microneedling.
Dr Lam Bee Lan, director of Ageless Medi-Aesthetics, told The New Paper: "Recombinant DNA technology is more efficient in producing large amounts of artificial messenger proteins effective for skin and hair renewal compared with stem cells derived from plants."
Methods of hair restoration are often divided into two broad categories - invasive techniques and topical and/or oral solutions. They can either be expensive or linked to side effects such as erectile dysfunction, ejaculatory dysfunction and loss of libido.
But Dr Lam cautioned that before treatments are prescribed, patients must consult with a physician to ascertain if they are suitable for them.
"Treatments based on recombinant DNA technology should be worked in as a first-line treatment when you start to experience more hair loss than usual, or as part of a regular routine in maintaining a full head of hair.
"For more severe hair loss, patients should consider a hair transplant," she said.
While there are minimal side effects such as occasional soreness and redness that will resolve within one to two hours, Dr Lam noted that most patients will experience slowing down of hair loss after the first session, while new hair will grow after the second session.
Home-grown scalp specialist PHS Hairscience has also explored stem cell technology and cell signalling technology since 2014 to treat hair loss or greying hair on the cellular level.
Ms Anita Wong, its chief executive and founder, told TNP: "As the body ages or changes due to reasons such as stress or lifestyle choices, cell functions can deteriorate, and cell activity that directly impacts new hair growth or melanin (hair pigment) production becomes less than optimal."
PHS Hairscience's marquee treatment, Miracle Stem Cell Solution, leverages on stem cell science and cell signalling to reactivate dormant follicle cells to promote hair growth. At $297 a session, it can be complemented with the FEM/HOM Thickening range of products.
She said: "These active botanical stem cells also work to increase the life span of hair follicles so your hair can remain in the anagen (growth) phase of the hair growth cycle for a longer period of time.
"Keeping the hair in this growth phase will maximise the length and thickness of new hair, as well as stop the existing strands from shedding."
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Turmeric: what are the benefits and is it good for you? – The Irish Times
Posted: October 30, 2019 at 1:48 pm
Have you noticed lattes, ice cream and smoothies with a tawny hue? That could be a sign of a not-so-secret ingredient: turmeric. The botanical is omnipresent in health food aisles, in the form of pills and powders.
Turmeric, native to South Asia, is one of the fastest-growing dietary supplements. In 2018, products racked up an estimated 300 million in sales in the United States, a more than sevenfold increase from a decade earlier, according to a report from Nutrition Business Journal.
Brightening up the pantries of many homes in India, the spice is interwoven into daily life, the cuisine, and cultural and healing traditions. A member of the ginger family, it has been used in ayurvedic medicine for thousands of years. Apply turmeric to wounds, and its believed to fight infection. Mix it with milk, and the mind calms. Tint the entrance of new homes with a paste to welcome prosperity.
Turmeric is auspicious and one of the most important herbs, said Anupama Kizhakkeveettil, a board member of the National Ayurvedic Medical Association.
Sliced open, or dried into a spice, the Curcuma longa plant imparts its amber colour and earthy, bitter flavour to food like curry. The active ingredient captured in many turmeric supplements is curcumin. Curcumin, along with the other curcuminoid compounds, compose only about 3 per cent of the dried spice.
And bottles will often say turmeric on the front but list curcumin in the ingredients.
Turmeric is hailed for helping a host of conditions: high cholesterol, hay fever, depression, gingivitis, premenstrual syndrome and even hangovers. In ayurvedic medicine, it is believed to act as an anti-viral, anti-bacterial and anti-parasitic, and has long been used to help with diabetes, pain, rheumatism, osteoarthritis, memory and skin conditions like eczema.
We use it for so many different conditions, its a time-tested herb, Kizhakkeveettil said. Unfortunately, our science doesnt fit into complete randomised controlled trials. That is alternative medicines biggest challenge.
Researchers sought to answer this by sifting through the available literature. In a 2017 paper in the Journal of Medicinal Chemistry, they concluded its fools gold. There are claims that it can cure everything, said Kathryn Nelson, a research assistant professor at the University of Minnesota and the studys lead author. To me, that is a red flag.
Dr Amit Garg, a professor of medicine at Western University in London, Ontario, knew about turmerics medicinal use because of his Indian heritage. He knew first hand of its rich cultural significance too: on his wedding day, his relatives rubbed the spice all over him because it is believed to be cleansing.
After seeing the effectiveness of curcumin, in smaller studies, Garg and his colleagues decided to test it on a larger scale in hopes it would make elective aortic surgery safer by reducing the risk of complications, which include heart attacks, kidney injury and death. In the randomised clinical trial that followed, about half of the 606 patients were administered 2,000 milligrams of curcumin eight times over for four days, while the others were given a placebo. It was a bit disappointing, but we couldnt demonstrate any benefit used in this setting, Garg said of the study, published last year in the Canadian Medical Association Journal.
In fact, there is not enough reliable evidence in humans to recommend turmeric or curcumin for any condition, according to the US National Center for Complementary and Integrative Health. Turmeric became a nutritional golden child partly because of its promise in laboratory studies cellular and animal. Some research indicates that both turmeric and curcumin, the active ingredient in turmeric supplements, have anti-inflammatory, antioxidant, anti-bacterial, anti-viral and anti-parasitic activity. But this has mostly been demonstrated in laboratory studies, and, in many cases, the benefits of preclinical research isnt observed in clinical trials.
According to Natural Medicines, a database that provides monographs for dietary supplements, herbal medicines, and complementary and integrative therapies, while some clinical evidence shows that curcumin might be beneficial for depression, hay fever, hyperlipidemia, ulcerative colitis, osteoarthritis and nonalcoholic fatty liver disease, its still too early to recommend the compound for any of these conditions.
And Natural Medicines has found there isnt enough good scientific evidence to rate turmeric or curcumins use for memory, diabetes, fatigue, rheumatoid arthritis, gingivitis, joint pain, PMS, eczema or hangovers.
Physicians say more research is needed. Dr Gary Small, a professor of psychiatry and biobehavioral sciences at the David Geffen School of Medicine at the University of California, Los Angeles, who studies curcumins effect on memory, sees a lot of therapeutic potential. He also states that existing research demonstrates curcumins biological effects.
What may be affecting curcumins efficacy, doctors say, is that it is poorly absorbed from the gastrointestinal tract. In Indian cooking, turmeric is usually heated in a fat, like oil, which can increase absorption. Certain supplement manufacturers are also taking steps to improve this curcumins bioavailability by combining the compound with other components. For instance, a chemical found in black pepper called piperine is sometimes added to curcumin supplements in proprietary blends to increase its absorption.
Researching curcumin can be challenging because some blends have better bioavailability than others, and varying amounts of the active ingredient. If you did the study over and over again but used slightly different preparations, you would probably have different results, said Dr Janet Funk, a professor of medicine at the University of Arizona College of Medicine, who studies curcumins effect on bone.
Still, even if absorption improved, curcumin would not have any biological effects, Nelson contends. Turmeric may still have health benefits, she said, but they just may be from another compound or combination of compounds.
Consuming it by mouth is safe, up to 2g of turmeric daily for a year, and 4g daily of curcumin for a month, according to Natural Medicines. Turmeric aficionados who also use it as a face mask can relax too; the database indicates it is most likely safe to apply to the skin.
Doctors recommend that patients tell a physician they are taking turmeric. High doses of turmeric and its isolated constituents can have some rather unpleasant side effects, including diarrhea and nausea. Curcumin may also interact with anti-coagulants and anti-platelets, antacids, and drugs used for chemotherapy and to control blood pressure. While the spice is considered safe in food, therapeutic doses should be avoided during pregnancy.
The US Food and Drug Administration does not test dietary supplements such as turmeric for safety and effectiveness but announced this year that it would improve oversight of the growing industry.
One study published in 2018 in Molecular Nutrition & Food Research, found that the cheaper the turmeric product, the more likely it was to have chemical compounds suggestive of synthetic curcumin; and products with turmeric root were more likely to have higher lead levels. One sample exceeded recommended limits for lead.
How about all those turmeric lattes? Doctorssay that sprinkling a little bit of the bitter spice into frothed milk doesnt have proven health benefits. But that doesnt mean it isnt delicious.
As for Garg, he is not closing the bottle cap on curcumin. To wit: he is in the middle of a randomised study with a different preparation and dosing to see if curcumin prevents the progression of kidney disease. There are still many promising things about curcumin and turmeric, he said. I remain open-minded. New York Times
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Turmeric: what are the benefits and is it good for you? - The Irish Times
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Reviewing Madrigal Pharmaceuticals Inc. (MDGL)’s and Brainstorm Cell Therapeutics Inc. (NASDAQ:BCLI)’s results – MS Wkly
Posted: October 30, 2019 at 1:46 pm
We will be contrasting the differences between Madrigal Pharmaceuticals Inc. (NASDAQ:MDGL) and Brainstorm Cell Therapeutics Inc. (NASDAQ:BCLI) as far as profitability, analyst recommendations, risk, institutional ownership, dividends, earnings and valuation are concerned. The two businesses are rivals in the Biotechnology industry.
Valuation & Earnings
Table 1 shows gross revenue, earnings per share (EPS) and valuation of the two companies.
Profitability
Table 2 shows us the return on assets, return on equity and net margins of both companies.
Volatility & Risk
Madrigal Pharmaceuticals Inc.s current beta is 1.16 and it happens to be 16.00% more volatile than Standard & Poors 500. Brainstorm Cell Therapeutics Inc.s 1.19 beta is the reason why it is 19.00% more volatile than Standard & Poors 500.
Liquidity
Madrigal Pharmaceuticals Inc. has a Current Ratio of 45.8 and a Quick Ratio of 45.8. Competitively, Brainstorm Cell Therapeutics Inc.s Current Ratio is 1 and has 1 Quick Ratio. Madrigal Pharmaceuticals Inc.s better ability to pay short and long-term obligations than Brainstorm Cell Therapeutics Inc.
Analyst Recommendations
The table shown features the ratings and recommendations for Madrigal Pharmaceuticals Inc. and Brainstorm Cell Therapeutics Inc.
$150.5 is Madrigal Pharmaceuticals Inc.s average target price while its potential upside is 57.59%. Meanwhile, Brainstorm Cell Therapeutics Inc.s average target price is $9, while its potential upside is 147.25%. Based on the results shown earlier, Brainstorm Cell Therapeutics Inc. is looking more favorable than Madrigal Pharmaceuticals Inc., analysts view.
Insider & Institutional Ownership
Institutional investors held 98.9% of Madrigal Pharmaceuticals Inc. shares and 11.4% of Brainstorm Cell Therapeutics Inc. shares. Insiders held roughly 11.33% of Madrigal Pharmaceuticals Inc.s shares. Comparatively, Brainstorm Cell Therapeutics Inc. has 0.6% of its share held by insiders.
Performance
Here are the Weekly, Monthly, Quarterly, Half Yearly, Yearly and YTD Performance of both pretenders.
For the past year Madrigal Pharmaceuticals Inc. has -22.56% weaker performance while Brainstorm Cell Therapeutics Inc. has 12.96% stronger performance.
Summary
Brainstorm Cell Therapeutics Inc. beats Madrigal Pharmaceuticals Inc. on 6 of the 10 factors.
Madrigal Pharmaceuticals, Inc., a clinical-stage biopharmaceutical company, focuses on the development and commercialization of therapeutic candidates for the treatment of cardiovascular, metabolic, and liver diseases. The companys lead candidate is MGL-3196, which is in Phase II clinical trials, a liver-directed thyroid hormone receptor- (THR-) agonist used for the treatment of nonalcoholic fatty liver disease, nonalcoholic steatohepatitis, and familial hypercholesterolemia. It is also developing MGL-3745, which is in pre-clinical stage, a THR- agonist that is in preclinical trials. The company was founded in 2011 and is headquartered in West Conshohocken, Pennsylvania.
Brainstorm Cell Therapeutics Inc., a biotechnology company, develops adult stem cell therapies for neurodegenerative disorders that include amyotrophic lateral sclerosis, multiple sclerosis, Parkinsons disease, and others. The company holds rights to develop and commercialize its NurOwn technology through a licensing agreement with Ramot of Tel Aviv University Ltd. Its NurOwn technology is based on a novel differentiation protocol, which induces differentiation of the bone marrow-derived mesenchymal stem cells into neuron-supporting cells and secreting cells that release various neurotrophic factors, including glial-derived neurotrophic factor, brain-derived neurotrophic factor, vascular endothelial growth factor, and hepatocyte growth factor for the growth, survival, and differentiation of developing neurons. The company was formerly known as Golden Hand Resources Inc. and changed its name to Brainstorm Cell Therapeutics Inc. in November 2004 to reflect its new line of business in the development of novel cell therapies for neurodegenerative diseases. Brainstorm Cell Therapeutics Inc. was founded in 2000 and is headquartered in Hackensack, New Jersey.
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Gene Therapy/Editing Series 1: A Brief Introduction To Gene Therapy – Seeking Alpha
Posted: October 30, 2019 at 1:46 pm
The recent approval of various gene therapies, for example, Luxturna and Zolgesma and high premium acquisitions of gene therapy companies have shifted the investor focus to this rapidly growing biotechnology field. In this series of review articles, I will review the gene therapy and gene editing field, starting first with the basics, including a brief overview of the history of the field and then moving on to some technical aspects, for example, the manufacturing, different methods of delivery, and then moving on to discussing the competitive landscape covering one genetic disease in each article.
Let's first define what is a gene? A gene is a sequence of nucleotides in DNA that encodes the synthesis of a gene product, which is usually a protein.
(F8 gene, mutations in the gene cause Hemophilia A)
Usually, the code (in the form of a specific arrangement of nucleotides or base pairs contained in the gene is used to form mRNA (called transcription) which acts as a messenger to take the code to the target organ of the body. The information stored in the mRNA is then used to encode and synthesize the target protein (called translation) which then performs its intended function in the body.
(Steps involved in synthesizing a protein from the code in a gene)
An estimated number of protein-coding genes in the human body is approximately 20,000 to 25,000, which has been revised down from the initial prediction of 100,000 genes. Each gene contains a number of base pairs, the number of which is estimated to range from about 50 million to 300 million in the human body. In general, a gene therapy can be broadly defined as delivering in a new gene into the cells to compensate for a defective gene. In gene therapy, a newly delivered gene can perform different functions; for example, it can either replace the defective gene or it can silence an abnormal gene.
(An example of a gene therapy using an adenoviral vector to deliver the normal gene)
While I will discuss the various steps and delivery systems in gene therapy in detail later, viruses like lentiviruses and adenovirus are most commonly used as vectors in gene therapy. It was as early as 1950s that scientists first discovered that a virus can be used to inject the DNA in the cells of the host. In 1970s, various experiments started to use viruses as delivery systems for genes in the human body. In 1971, Merril, et al conducted a scientific experiment showing that DNA could be injected into the human cells to fix a biological problem in the cells. This group of scientists extracted the cells from patients suffering from a disease called Galactosemia. It is important to note that this first gene therapy experiment involves the manipulation of genes ex vivo, that is in cells growing in a petri dish outside the body in a lab, which is easier to perform than manipulating the genes inside the human body, called in vivo approach. In 1972, a famous article in the prestigious journal Science by authors Friedman and Roblin first proposed that the gene therapy may ameliorate some human genetic diseases in the future. During the 1980s, various scientists like Martin Cline and French Anderson conducted experiments on using viruses as delivery vehicles for DNA in human or mouse cells. The first human trials of gene therapy started in the late 1980s and the results were reported in early 1990s. One of the first reported clinical studies in humans involved ex vivo modification of white blood cells taken from patients with advanced melanoma, using a retroviral vector to insert a gene coding for interleurkin-2 and injecting the genetically altered cells back into the patients. During the 1990s, French Anderson reported a successful clinical trial where a retroviral vector was used to transfer a gene encoding for adenosine deaminase, ADA in children with severe combined immunodeficiency, SCID. During the 1990s, most of the work in gene therapy continued in the therapeutic area of ADA-SCID.
Despite reasonably successful clinical results, the field of gene therapy suffered a serious setback in 1999. Jesse Gelsinger, an 18-year-old patient with a disease called ornithine transcarbamylase, OTC deficiency, which results due to a missing gene coding OTC died 4 days after receiving the gene therapy in a clinical trial conducted by the University of Pennsylvania due to massive immune response resulting in multi-organ failure. As a result, FDA put a suspension on various gene therapy clinical trials.
The field of gene therapy was then suspended for almost a decade. Glybera, a gene therapy was approved in Europe for reading a genetic disease, lipoprotein lipase deficiency in 2012. However, Glybera was a commercial failure after insurers in Europe were reluctant to pay for its expensive $1 million per patient tag. Finally, uniQure (QURE) the company that developed Glybera discontinued it.
Another commercial gene therapy failure was Strimvelis, a stem cell gene therapy to treat ADA-SCID. Despite its price being lower than Glybera ($665,000 per year), the therapy was not commercially successful in Europe and was sold by GlaxoSmithKline (GSK) to Orchard Therapeutics (ORTX) in 2018. In the US, the first approved gene therapy was Kymriah, an autologous CAR-T therapy to treat autologous lymphoblastic leukemia (ALL), which was developed by Novartis (NYSE:NVS).
After Kymriah, another autologous CAR-T therapy, Yeskarta (by Kite Pharmaceuticals) was approved by FDA to treat adult diffuse large B-cell lymphoma. Kite was later acquired by Gilead (NASDAQ:GILD). The first in vivo gene therapy approval in the US was Luxturna, an AAV gene therapy for patients with RPE 65 mutation-associated retinal dystrophy, which was developed by Spark Therapeutics which also was later acquired. Luxturna was another major milestone in the history of gene therapy as it resulted in a miraculous effect of restoring vision to children who were blind since birth. Recently, bluebird bio's (BLUE) gene therapy for transfusion-dependent beta-thalassemia was approved in Europe.
The developmental landscape of gene therapies can be summarized in some excellent figures from the journal Molecular Therapy published by the American Society of Gene and Cell Therapy (ASGCT). A group of researchers reviewed the medical literature and identified 336 gene therapies being developed for 138 different clinical indications covering 165 genetic targets excluding oncology. The researchers found that 74% of these 336 gene therapies were concentrated in five medical specialties, that is, hematology, endocrinology, neurosciences, cardiology, and ophthalmology. When classifying by different disease families, inborn errors of metabolism was the disease category with a majority of ongoing gene therapy trials.
(Landscape of gene therapy programs by organ system and disease area, source: Mol. Therapy)
When looking at specific clinical indications, Duchenne muscular dystrophy (DMD) was the clinical indication with the highest number of gene therapies being developed (15). HIV gene therapies (12 gene therapy programs) and hemophilia (11 gene therapy programs) took the second and third place respectively.
In terms of the number of gene therapy/editing programs being developed by a particular company or organization, Sangamo Therapeutics (SGMO) took the top spot (see the figure below).
(Landscape of gene therapy programs by company/organization, source: Mol. Therapy)
In conclusion, gene therapy has recovered from its earlier setbacks to emerge as one of the most innovative areas in biotechnology. In this first article of the series, I have provided a brief background about gene therapy, its history, and a broad top-down landscape. In the next article in the premium service, I will discuss various delivery systems for gene therapy.
A free two-week trial for the premium Marketplace service is open for another week only. Only 25 more spots left.
Disclosure: I am/we are long BLUE, ORTX, QURE, SGMO, AXGT, CRSP. I wrote this article myself, and it expresses my own opinions. I am not receiving compensation for it (other than from Seeking Alpha). I have no business relationship with any company whose stock is mentioned in this article.
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Anika Therapeutics, Inc. (ANIK)’s Stock Is Buy After Today’s Significant Increase – The Lamp News
Posted: October 30, 2019 at 1:45 pm
Investors sentiment decreased to 1.4 in Q2 2019. Its down 0.37, from 1.77 in 2019Q1. It turned negative, as 16 investors sold Anika Therapeutics, Inc. shares while 42 reduced holdings. 35 funds opened positions while 46 raised stakes. 13.49 million shares or 3.81% more from 13.00 million shares in 2019Q1 were reported.Moreover, South Dakota Council has 0.05% invested in Anika Therapeutics, Inc. (NASDAQ:ANIK). 218,686 are held by Geode Cap Mgmt. Nelson Van Denburg And Campbell Wealth Group Ltd accumulated 13,306 shares or 0.1% of the stock. Oaktop Ii Lp owns 12,500 shares or 0.11% of their US portfolio. Thrivent For Lutherans holds 0% or 11,149 shares. 5,435 are owned by Jefferies Gru Limited Liability Corporation. Everence Cap Mngmt Incorporated accumulated 0.04% or 6,520 shares. Moreover, Deutsche Bank & Trust Ag has 0% invested in Anika Therapeutics, Inc. (NASDAQ:ANIK). Aqr Limited Com reported 6,013 shares stake. Glenmede Co Na holds 54 shares. The Illinois-based Nuveen Asset Mgmt Llc has invested 0% in Anika Therapeutics, Inc. (NASDAQ:ANIK). State Board Of Administration Of Florida Retirement owns 11,873 shares. Mark Sheptoff Finance Planning Ltd Limited Liability Company, a Connecticut-based fund reported 300 shares. Voloridge Invest Management Ltd holds 0.01% or 6,610 shares. Foundry Prtnrs Lc accumulated 0.09% or 54,915 shares.
The stock of Anika Therapeutics, Inc. (NASDAQ:ANIK) is a huge mover today! The stock increased 32.45% or $17.61 during the last trading session, reaching $71.88. About 498,503 shares traded or 144.39% up from the average. Anika Therapeutics, Inc. (NASDAQ:ANIK) has risen 39.72% since October 25, 2018 and is uptrending. It has outperformed by 39.72% the S&P500.The move comes after 6 months positive chart setup for the $990.72M company. It was reported on Oct, 25 by Barchart.com. We have $78.35 PT which if reached, will make NASDAQ:ANIK worth $89.16 million more.
More notable recent Anika Therapeutics, Inc. (NASDAQ:ANIK) news were published by: Benzinga.com which released: 42 Stocks Moving In Tuesdays Pre-Market Session Benzinga on July 30, 2019, also Seekingalpha.com with their article: Anika up 35% after Q2 beat Seeking Alpha published on July 25, 2019, Seekingalpha.com published: Pluristem Therapeutics and EDAP TMS among healthcare gainers; Align Technology among losers Seeking Alpha on July 25, 2019. More interesting news about Anika Therapeutics, Inc. (NASDAQ:ANIK) were released by: Benzinga.com and their article: The Daily Biotech Pulse: Setback For Bristol-Myers Squibb, Gemphire Explodes, Lillys Nasal Low Blood Sugar Drug Benzinga published on July 25, 2019 as well as Finance.Yahoo.coms news article titled: Heres What Anika Therapeutics, Inc.s (NASDAQ:ANIK) P/E Is Telling Us Yahoo Finance with publication date: August 23, 2019.
Anika Therapeutics, Inc., together with its subsidiaries, provides orthopedic medicines for patients with degenerative orthopedic diseases and traumatic conditions in the United States and internationally. The company has market cap of $990.72 million. The firm develops, makes, and commercializes therapeutic products based on its proprietary hyaluronic acid technology. It has a 35.24 P/E ratio. The Companys orthobiologics products comprise ORTHOVISC, ORTHOVISC mini, MONOVISC, and CINGAL for the treatment of osteoarthritis of the knee; HYALOFAST, a biodegradable support for human bone marrow mesenchymal stem cells used for cartilage regeneration and as an adjunct for microfracture surgery; HYALONECT, a woven gauze used as a bone graft wrap; HYALOSS used to mix blood/bone grafts to form a paste for bone regeneration; and HYALOGLIDE, an ACP gel used in tenolysis treatment.
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Anika Therapeutics, Inc. (ANIK)'s Stock Is Buy After Today's Significant Increase - The Lamp News
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Stem Cell Therapy Market Trends, Secondary Research With Geron Corporation, Vericel Corporation, Pluristem Therapeutics, Cytori Therapeutics, Fate…
Posted: October 30, 2019 at 1:44 pm
Stem Cell Therapy Market research analysis and insights displayed in this report are very thoughtful for the businesses to make enhanced decisions, to build up better strategies about production, marketing, sales and promotion of a particular product. Stem Cell Therapy market report also takes into consideration several major factors such as revenue, cost, gross and gross margin while analysing market data. Various markets at local, regional and international level are thought of in this Stem Cell Therapy report. All this helps in extending their reach towards the success. The use of advanced tools and techniques applied for this report makes it the premium in the class. By understanding clients needs precisely, this report merges business and product information for the sustainable growth in the market. Geron Corporation, Vericel Corporation, Pluristem Therapeutics, Cytori Therapeutics, Fate Therapeutics are some players grooming the market.
Stem Cell Therapy Market is expected to reach USD 15.63 billion by 2025, from USD 7.72 billion in 2017 growing at a CAGR of 9.2% during the forecast period of 2018 to 2025. The Stem Cell Therapy market report contains data for historic year 2016, the base year of calculation is 2017 and the forecast period is 2018 to 2025 (Updated values listed in sample report).
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Stem cell therapy is the therapy which uses stem cells for the treatment or prevention of a disease. Bone marrow transplant is the widely applicable therapy which is followed by umbilical cord blood. Research is going on to develop various sources (such as cord blood cells, bone marrow and skin) to use these cells for treatment of various disorders like neurodegenerative diseases and conditions such as heart disease, diabetes and other conditions. Some of the major players operating in the global stem cell therapy market are
Others: ViaCyte, Inc, AbbVie, Mesoblast Ltd., Roslin Cells, Regeneus Ltd, ReNeuron Group plc,, International Stem Cell Corporation, Aastrom Biosciences, Inc., Advanced Cell Technology, Cryo Cell International, Cytori Therapeutics, Inc., Geron Corporation, and Invitrogen and others. The global stem cell therapy market is highly fragmented and the major players have used various strategies such as new product launches, expansions, agreements, joint ventures, partnerships, acquisitions, and others to increase their footprints in this market. The report includes market shares of the global stem cell therapy market for global, Europe, North America, Asia Pacific and South America.
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Major Market Drivers and Restraints:
Drivers:
Restraints:
Segmentation:
The global stem cell therapy market is segmented based on
Type
Product
Application
End Users
Geographical Segments
On the basis of type, the market is segmented into
Allogeneic stem cell therapy
Autologous stem cell therapy
The allogeneic stem cell therapy segment is expected lead the market because of commercialization of allogeneic stem cell therapy products and wide application with easy scale up process.
Based on products, the market is segmented into
Adult stem cells
Human embryonic stem cells
Induced pluripotent stem cells and others
The adult stem cells accounts highest share in market due to ability to generate trillions of specialized cells which may lower the risks of rejection and repair tissue damage.
Based on application, the market is segmented into
Musculoskeletal disorders
Wounds and injuries
Cardiovascular diseases
Surgeries
Gastrointestinal diseases, and other applications
The musculoskeletal disorders segment leads the market due to availability of stem cell-based products for the treatment of musculoskeletal disorders, high prevalence of musculoskeletal disorders and bone & joint diseases.
Based on end users, the market is segmented into
Therapeutic companies
Cell and tissues banks
Tools and reagent companies
Service companies
The growing number of stem cell donors, improved stem cell banking facilities and because of the research and development therapeutic companies held the largest share in stem cell therapy.
By Geography
North America (U.S., Canada, Mexico)
South America (Brazil, Argentina, Rest of South America)
Europe (Germany, France, United Kingdom, Italy, Spain, Russia, Turkey, Belgium, Netherlands, Switzerland, Rest of Europe)
Asia-Pacific ( Japan, China, South Korea, India, Australia, Singapore, Thailand, Malaysia, Indonesia, Philippines, Rest of Asia Pacific)
Middle East & Africa (South Africa, Egypt, Saudi Arabia, United Arab Emirates, Israel, Rest of Middle East & Africa)
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